Progression After Molecular Targeted Agents: Hepatic Arterial Changes and Transarterial Chemoembolization in

Noritaka Matsuda1, Norihiro Imai2, Teiji Kuzuya3

  • 1Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Aichi, Japan.

In Vivo (Athens, Greece)
|February 24, 2021
PubMed
Abstract

Insights

Molecular targeted agent (MTA) treatment significantly reduced hepatic artery diameters in hepatocellular carcinoma (HCC) patients, suggesting ischemia. Transarterial chemoembolization (TACE) after MTA is safe but offers limited therapeutic benefit.

Area of Science:

  • Hepatobiliary imaging and intervention
  • Oncology
  • Vascular radiology

Background:

  • Hepatocellular carcinoma (HCC) management often involves multimodal therapy.
  • Molecular targeted agents (MTAs) are increasingly used in HCC treatment.
  • Transarterial chemoembolization (TACE) is a standard locoregional therapy for HCC.

Purpose of the Study:

  • To assess changes in hepatic artery diameters following MTA treatment in HCC patients.
  • To evaluate the safety and efficacy of TACE as a subsequent treatment after MTA in HCC.
  • To investigate the impact of MTA on the vascularity of HCC.

Main Methods:

  • Retrospective analysis of 33 intermediate HCC patients treated with MTA and TACE.
  • Evaluation of hepatic artery, splenic artery, and portal vein diameters before and after MTA.
  • Assessment of TACE safety and therapeutic effect post-MTA treatment.

Main Results:

  • Significant decrease in hepatic artery diameters after long-term MTA treatment.
  • No significant changes observed in splenic artery or portal vein diameters.
  • TACE following MTA was safe, with no major adverse events, but showed limited therapeutic efficacy.

Conclusions:

  • MTA treatment leads to hepatic artery narrowing, indicating ischemic effects and potential tumor vessel normalization.
  • TACE can be safely administered after MTA without compromising hepatic reserve.
  • The therapeutic benefit of TACE is diminished when used after MTA in HCC treatment.